Anyone have any advice as to how or where to sell a rife machine?? I bought it a couple of years ago and never used it... any thoughts would be greatly appreciated.... thanks, Laura
Posted by Keebler (Member # 12673) on :
- I'd start close to home.
You might contact your local and state Lyme Support Groups. I know there is a very active Minnesota Lyme group. If you "do" Facebook, they have a Facebook page.
If you have a LLMD or LL ND, also let their office know as they might be able to share this information.
Beyond that, I'm sure others will reply with suggestions. -
Posted by Lymetoo (Member # 743) on :
Aware that just about everyone needs cash rather than some item that is not being used, but even if you are not using rife now, I just hate to see you sell it as it could come in very handy at some other time.
Rife is helpful for so much more than lyme, too.
So other than needing the money now - or maybe having a pacemaker and therefore being unable to use a rife machine . . . please keep in mind that it could serve you well into the future, and for those in your family, too.
Take a look at the CAFL list. So many other infections / conditions that rife can help address. Even just the 10K frequency for inflammation can be very nice and is okay to used daily. -
Posted by droid1226 (Member # 34930) on :
what model is it?
Posted by luluMN (Member # 12703) on :
Thanks Keebler...I just had such bad reactions to it that it has left a very bad impression on me...others have told me this also, guess Im a slow learner tho...
Posted by luluMN (Member # 12703) on :
Droid~ Its a EMEM 5a...
Posted by Keebler (Member # 12673) on :
- lulu,
"Bad reactions" can be due to the time, frequency, whether liver support was adequate &/or if binders (particular supplements) were adequate for heavy metals that can be released by spirochetes as they are targeted.
Much of this is detailed in Rosner's book. Now, you may have considered all that but just in case not, worth a thought.